Linked Data
ClinVar Variation Id:
496885
dbSNP Id:
rs149163661
ExAC:
6:51524065 C / T
gnomAD v2:
6-51524065-C-T
gnomAD v3:
6-51659267-C-T
gnomAD v4:
6-51659267-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.51659267C>T , CM000668.2:g.51659267C>T | GRCh38 |
| NC_000006.11:g.51524065C>T , CM000668.1:g.51524065C>T | GRCh37 |
| NC_000006.10:g.51632024C>T | NCBI36 |
| NG_008753.1:g.433359G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371117.8:c.10859G>A MANE Select | ENSP00000360158.3:p.Arg3620His | |
| ENST00000371117.7:c.10859G>A | ENSP00000360158.3:p.Arg3620His | |
| NM_138694.3:c.10859G>A | NP_619639.3:p.Arg3620His | |
| XM_011514679.1:c.10859G>A | XP_011512981.1:p.Arg3620His | |
| XM_011514680.1:c.10859G>A | XP_011512982.1:p.Arg3620His | |
| XM_011514681.1:c.10730G>A | XP_011512983.1:p.Arg3577His | |
| XM_011514682.1:c.10721G>A | XP_011512984.1:p.Arg3574His | |
| XM_011514683.1:c.10217G>A | XP_011512985.1:p.Arg3406His | |
| XM_011514684.1:c.10148G>A | XP_011512986.1:p.Arg3383His | |
| XM_011514687.1:c.10157-10047G>A | XP_011512989.1:n.10157-10047G>A | |
| XM_011514690.1:c.4934G>A | XP_011512992.1:p.Arg1645His | |
| XM_011514691.1:c.4934G>A | XP_011512993.1:p.Arg1645His | |
| XR_926870.1:n.535+6894C>T | ||
| XR_926871.1:n.403+6894C>T | ||
| XR_926872.1:n.535+6894C>T | ||
| XM_011514680.3:c.10859G>A | XP_011512982.1:p.Arg3620His | |
| XM_011514682.3:c.10721G>A | XP_011512984.1:p.Arg3574His | |
| XM_011514683.3:c.10217G>A | XP_011512985.1:p.Arg3406His | |
| XM_011514684.3:c.10148G>A | XP_011512986.1:p.Arg3383His | |
| XM_011514690.3:c.4934G>A | XP_011512992.1:p.Arg1645His | |
| XM_011514691.3:c.4934G>A | XP_011512993.1:p.Arg1645His | |
| XM_017010944.2:c.10859G>A | XP_016866433.1:p.Arg3620His | |
| XM_017010945.2:c.10784G>A | XP_016866434.1:p.Arg3595His | |
| XM_017010946.2:c.10664G>A | XP_016866435.1:p.Arg3555His | |
| XM_017010947.2:c.10595G>A | XP_016866436.1:p.Arg3532His | |
| XM_017010948.2:c.10148G>A | XP_016866437.1:p.Arg3383His | |
| XM_017010949.2:c.8999G>A | XP_016866438.1:p.Arg3000His | |
| XR_001743469.1:n.11135G>A | ||
| XR_001744157.1:n.3145+6894C>T | ||
| XR_926870.2:n.3145+6894C>T | ||
| XR_926871.2:n.3013+6894C>T | ||
| XR_926872.2:n.3145+6894C>T | ||
| NM_138694.4:c.10859G>A MANE Select | NP_619639.3:p.Arg3620His |